liquid culture method 中文意思是什麼

liquid culture method 解釋
液體培養法
  • liquid : n 1 液體。2 【語言學】流音〈如 [l] [r]〉 adj 1 液體的，液態的，流動的。2 清澄的，透明的。3 易變的...
  • culture : n. 1. 教養；修養；磨煉。2. 文化，（精神）文明。3. 人工培養，養殖；培養菌，培養組織。4. 耕作；栽培；造林。vt. 使有教養。
  • method : n 1 方法，方式；順序。2 （思想、言談上的）條理，規律，秩序。3 【生物學】分類法。4 〈M 〉【戲劇】...
  1. This experiment passing to grope for the carbon source constitutes of the culture medium and using t. reesei rut c - 30 induced the expression of # - mannanase ( # - 1, 4 - mannan mannohydrolase ec 3. 2. 1. 78 ). in this experiment i put the constant carbon source ( lactose and locust bean gum ) in the foundation culture medium ( mandels nourishment liquid ) of t. reesei rut c - 30, then proceeded the variable carbon source ( dragon spruce fiber, com rush pith fiber, wheat straw fiber, wheat straw xylan, corn rush pith xylan, dragon spruce mannan ) to single factor, double factor, three factor, four factor and five factor orthogonal experiment. 1 determined the activity of p - mannanase using locost bean gum as substract by the 3, 5 - dinitosalicylic acid method, and observed the growing situation of the gernic at the end i selected the directions for the inducement expression of the # ? mannanase from trichoderma reesei rut - c30 that contained the dragon spruce fiber, wheat straw xylan, dragon spruce mannan

    在里氏木霉rutc - 30的基礎培養基（ mandels營養液）中加入固定碳源乳糖和槐豆膠，然後將可變碳源（雲杉纖維、玉米芯纖維、麥桿纖維、麥桿木聚糖、玉米芯木聚糖、雲杉甘露聚糖）進行單因子、雙因子、三因子、四因子、五因子的里氏木霉rutc - 30正交培養實驗，並以槐豆膠為底物用3 ， 5二硝基水楊酸法測定培養液中?甘露聚糖酶的活力。從而確定了酶活最高且菌體生長良好的含雲杉纖維、麥桿木聚糖和雲杉甘露聚糖的誘導培養基為最佳培養基，用該培養基培養的里氏木霉（ t . reesei ） rutc - 30使其轉錄的-甘露聚糖酶（ - 1 ， 4 - mannanmannohydrolaseec3 . 2 . 1 . 78 ） mrna量能夠滿足rt - pcr的要求。
  2. It was found that b - 6 isolated by the method of distinct zone of clearing in cellulose - congo red agar medium combined with measuring the enzyme activity of liquid culture filtrates had comparatively higher cellulase activity. by measuring activity of cellulase of strains growing in medium with different carbon sources and of washed mycelium induced by different carbon sources in certain time, it found that the formation of cellulase was regulated by the nature of the carbon source used for b - 6 and as3. 3711

    真菌纖維素酶是一種誘導酶，碳源同時也是主要的誘導物來源，為了研究碳源對真菌纖維素酶合成的誘導機理，本文利用液體生長培養和洗滌菌絲誘導培養法研究了不同碳源對兩菌株的誘導特性，並用電泳分析法研究了不同碳源的誘導酶譜。
  3. Edible gelatine. detection of coliforms. 30 degrees c culture method on liquid selective medium

    食用明膠.大腸桿菌的檢測.在30時液體選擇培養基的培養法
  4. Edible gelatine. determination of fecal coliforms. 44, 5 degrees c culture method on liquid selective medium

    食用明膠.糞便中大腸桿菌的檢測.在44 . 5時液體選擇培養基的培養法
  5. In order to investigate the tolerance of ectomycorrhizal fungi to heavy metals in vitro, three culture methods, namely liquid culture without agitation, liquid culture with agitation and solid agar culture, were investigated to determine which method would give the best combination of fungal biomass and ec50. the results indicated that liquid medium without agitation was the best culture method

    為研究外生菌根真菌本身對重金屬污染的耐性，比較了液體靜置、液體搖床和瓊脂固體培養這三種常用的菌絲體的純培養方法，以真菌生物量大小和分離難易程度為主要指標，篩選出液體靜置方法為最優方法。
  6. Testing water. enumeration of e. coli. miniaturised method by culture in liquid media

    水試驗. e . coli大腸桿菌計數.液體介質培養的小型方法
  7. M. p. n. testing water - detection and enumeration of coliforms and thermotolerant coliforms - general method by culture in liquid media m. p. n.

    水的測試.大腸桿菌和耐熱大腸桿菌的檢測和計數.液體介質中培養的一般方法
  8. Applied constant keeper can enable the microorganism to continuously culture in double periods of “ constant flowing method speed ”. ? it has a process as such : according to the multiplying speed that the bacteria cultures in double growing periods, and the speed that it consumes the nutritious material, fresh culturing liquid is continuously added. ? at the same time, the same amount of well - cultured bacteria liquid is continuously drawn out, so that the next two items are kept relatively constant : the added material and the consuming material ; the amount that the bacteria have multiplied and that has been drawn out

    應用恆化器，能使微生物以對數期「恆流法速度」連續培養，即根據菌種在對數生長期繁殖的速度和消耗營養物質的速度，不斷加入新鮮培養液，同時不斷抽出等量培養好的菌液，使加入物與消耗物、細胞繁殖量與細胞物質抽出量，保持相對穩定均恆。
分享友人
分享到 Line

分享到臉書